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Oral Pregabalin Premedication for Postoperative Pain Relief

Primary Purpose

Gynecologic Disease

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
placebo capsule (vitamin c)
Group pregabalin 150
Group pregabalin 300
Sponsored by
Zagazig University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gynecologic Disease focused on measuring Oral Pregabalin, Postoperative Pain Relief, Gynecological Surgeries

Eligibility Criteria

21 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Physical status: ASA I-II
  • BMI ≥ 20kg/m2 & ≤ 35kg/m2,
  • Written informed consent from the patient.

Exclusion Criteria:

  • Patients with known history of allergy to study drugs,
  • Patients on ACE inhibitors, anticonvulsant therapy or any drug interacting with pregabalin,
  • Patients on chronic alcohol, opioid, tranquilizer or sedative use,
  • Patient with renal impairment or heart failure,
  • Pregnant females, Psychological, mental disorders or depression,
  • Patients receiving anticoagulants therapy or suspected coagulopathy,
  • Patients already on pregbalin or gabapentin therapy.

Sites / Locations

  • faculty of medicine, Zagazig universityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Arm Label

control group

Group Pregabalin 150

Group Pregabalin 300

Arm Description

the patient will receive one placebo capsule (vitamin c) once one hour before the operation.

the patient will receive one capsule of pregabalin 150 mg once one hour before the operation

the patient will receive one capsule of pregabalin 300 mg once one hour before the operation

Outcomes

Primary Outcome Measures

changes in Postoperative pain
will be assessed by visual analogue scale (VAS), On a scale of 0-10, the patient will learn to quantify postoperative pain where 0= No pain and 10= Maximum worst pain.

Secondary Outcome Measures

The level of sedation
using the modified Ramsay Sedation Score: Patient is anxious and agitated or restless, or both. Patient is cooperative, oriented and tranquil. Patient responds to commands only. Patient exhibits brisk response to light glabellar tap or loud auditory stimulus. Patient exhibits sluggish response to light glabellar tap or loud auditory stimulus. Patient exhibits no response.
Total amount of rescue analgesic
Total amount of rescue analgesic requirement by the patient

Full Information

First Posted
November 23, 2020
Last Updated
September 2, 2021
Sponsor
Zagazig University
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1. Study Identification

Unique Protocol Identification Number
NCT04708353
Brief Title
Oral Pregabalin Premedication for Postoperative Pain Relief
Official Title
Effect of Two Different Doses of Oral Pregabalin Premedication for Postoperative Pain Relief After Gynecological Surgeries
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 20, 2020 (Actual)
Primary Completion Date
October 2021 (Anticipated)
Study Completion Date
November 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zagazig University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Pain management after gynecological surgeries is essential for early mobilization of the patient, decrease postoperative complication and hospital stay. The use of opioids is associated with adverse effects such as nausea, vomiting, ileus, pruritus, sedation and respiratory depression. Previous studies stated that pregabalin has been used to reduce pre-operative anxiety, acute postoperative pain, postoperative opioid requirements, postoperative nausea, vomiting and postoperative delirium. The most effective dose of pregabalin to relief postoperative pain with least side effect is still under trial. In this study we will compare between two different doses of pregabalin when given as oral premedication in patients undergoing gynecological surgeries under spinal anesthesia regarding postoperative pain in order to reduce opioids consumption and subsequently avoid opioid-related adverse effects.
Detailed Description
Postoperative pain, nausea and vomiting continue to be one of the most common and unpleasant complications after surgery. The traditional pain treatment with opioids alone is not adequate any more. To optimize pain treatment and postoperative outcome, new analgesics and new combination of already existing analgesics are searched for. Pain after gynecological surgery usually severe. Uncontrolled acute post-operative pain is associated with dissatisfaction, post-operative complications and considered as a strong risk factor for development of chronic pain. An enhanced recovery pathway for gynecological surgery must include a strategy to effectively control post-operative pain and allow attainment of other Enhanced Recovery After Surgery (ERAS) targets such as early mobilization and return to oral diet whilst reducing the need for opiates. Beyond increasing the risk of developing opioid use disorder, perioperative opioid consumption may produce undesirable side effects such as nausea, vomiting, constipation, ileus, pruritus, altered mental status, urinary retention, respiratory complications and increased length of hospital stay. While many of these side effects are frustrating to patient in the immediate postoperative period, the most dangerous effects are those that affect the respiratory system such as opioid-induced respiratory depression (ORD) which consider as a significant cause of brain damage and death in the postoperative period. Opioid reduction strategies prove useful for decreasing total opioid dose and, in turn, their associated adverse effects. Such strategies may include adjuvant non opioid analgesics such as α-2 agonists, gabapentinoids and N-methyl-D-aspartate receptor agonists as well as local, regional or neuraxial anesthesia and modification of surgical technique where possible for operative patients. Pregabalin is a new synthetic molecule and a structural derivative of the inhibitory neurotransmitter gamma-amino butyric acid. It is a α2-δ ligand that has analgesic, anticonvulsant, anxiolytic and sleep-modulating activities. Pregabalin binds potently to the α2-δ subunit of calcium channels, resulting in a reduction in the release of several neurotransmitters including glutamate, noradrenaline, serotonin, dopamine and substance P. Pregabalin could reduce the hyperexcitability of dorsal horn neurons induced by tissue damage; therefore it may be useful in the postsurgical pain prevention. In 2015, a meta-analysis published in British Medical Journal (BMJ) suggested that pregabalin could improve postoperative analgesia and opioid-related adverse effects namely, vomiting and visual disturbances after surgery. However, the use of the pregabalin for acute postoperative pain is still under trial though widely reported.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gynecologic Disease
Keywords
Oral Pregabalin, Postoperative Pain Relief, Gynecological Surgeries

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The patients will be allocated randomly using computer generated randomization table into three equal groups
Masking
ParticipantOutcomes Assessor
Masking Description
double-blinded ( patient and outcome assessors)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
control group
Arm Type
Placebo Comparator
Arm Description
the patient will receive one placebo capsule (vitamin c) once one hour before the operation.
Arm Title
Group Pregabalin 150
Arm Type
Active Comparator
Arm Description
the patient will receive one capsule of pregabalin 150 mg once one hour before the operation
Arm Title
Group Pregabalin 300
Arm Type
Active Comparator
Arm Description
the patient will receive one capsule of pregabalin 300 mg once one hour before the operation
Intervention Type
Drug
Intervention Name(s)
placebo capsule (vitamin c)
Intervention Description
the patient will receive one placebo capsule (vitamin c) once one hour before the operation
Intervention Type
Drug
Intervention Name(s)
Group pregabalin 150
Other Intervention Name(s)
p150
Intervention Description
the patient will receive one capsule of pregabalin 150 mg once one hour before the operation
Intervention Type
Drug
Intervention Name(s)
Group pregabalin 300
Other Intervention Name(s)
p300
Intervention Description
the patient will receive one capsule of pregabalin 300 mg once one hour before the operation
Primary Outcome Measure Information:
Title
changes in Postoperative pain
Description
will be assessed by visual analogue scale (VAS), On a scale of 0-10, the patient will learn to quantify postoperative pain where 0= No pain and 10= Maximum worst pain.
Time Frame
at 2, 4, 6, 8, 10, 12, 16, 20 and 24 hours postoperatively
Secondary Outcome Measure Information:
Title
The level of sedation
Description
using the modified Ramsay Sedation Score: Patient is anxious and agitated or restless, or both. Patient is cooperative, oriented and tranquil. Patient responds to commands only. Patient exhibits brisk response to light glabellar tap or loud auditory stimulus. Patient exhibits sluggish response to light glabellar tap or loud auditory stimulus. Patient exhibits no response.
Time Frame
at 2, 4, 6, 8, 10, 12, 16, 20 and 24 hours postoperatively
Title
Total amount of rescue analgesic
Description
Total amount of rescue analgesic requirement by the patient
Time Frame
in the first 24 hours

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Female patients scheduled for benign gynecological surgeries (abdominal hysterectomy, myomectomy, adnexal mass or disturbed ectopic pregnancy) under spinal anesthesia.
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Physical status: ASA I-II BMI ≥ 20kg/m2 & ≤ 35kg/m2, Written informed consent from the patient. Exclusion Criteria: Patients with known history of allergy to study drugs, Patients on ACE inhibitors, anticonvulsant therapy or any drug interacting with pregabalin, Patients on chronic alcohol, opioid, tranquilizer or sedative use, Patient with renal impairment or heart failure, Pregnant females, Psychological, mental disorders or depression, Patients receiving anticoagulants therapy or suspected coagulopathy, Patients already on pregbalin or gabapentin therapy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Asmaa M Galal, MD
Phone
01271550089
Ext
002
Email
asmaa_galal79@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rehab A Wahdan, MD
Phone
01003481323
Ext
002
Email
obz13w@yahoo.com
Facility Information:
Facility Name
faculty of medicine, Zagazig university
City
Zagazig
State/Province
Elsharqya
ZIP/Postal Code
44519
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Howaida A Kamal, MD
Phone
01225096755
Ext
002
Email
k.howaida@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
planned after the completion of the study and publication
IPD Sharing Time Frame
planned after the completion of the study and publication
IPD Sharing Access Criteria
principal investigator
Citations:
PubMed Identifier
16503325
Citation
Guay DR. Pregabalin in neuropathic pain: a more "pharmaceutically elegant" gabapentin? Am J Geriatr Pharmacother. 2005 Dec;3(4):274-87.
Results Reference
background
PubMed Identifier
15352959
Citation
Dahl JB, Mathiesen O, Moiniche S. 'Protective premedication': an option with gabapentin and related drugs? A review of gabapentin and pregabalin in in the treatment of post-operative pain. Acta Anaesthesiol Scand. 2004 Oct;48(9):1130-6. doi: 10.1111/j.1399-6576.2004.00484.x.
Results Reference
background
PubMed Identifier
25209095
Citation
Mishriky BM, Waldron NH, Habib AS. Impact of pregabalin on acute and persistent postoperative pain: a systematic review and meta-analysis. Br J Anaesth. 2015 Jan;114(1):10-31. doi: 10.1093/bja/aeu293. Epub 2014 Sep 10.
Results Reference
background
PubMed Identifier
22459341
Citation
Balaban F, Yagar S, Ozgok A, Koc M, Gullapoglu H. A randomized, placebo-controlled study of pregabalin for postoperative pain intensity after laparoscopic cholecystectomy. J Clin Anesth. 2012 May;24(3):175-8. doi: 10.1016/j.jclinane.2011.06.027. Epub 2012 Mar 28.
Results Reference
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Oral Pregabalin Premedication for Postoperative Pain Relief

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